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TAP: a targeted clinical genomics pipeline for detecting transcript variants using RNA-seq data

Published Online: 2018-09-10

Published Print: 2018-12

Authors

Chiu, Readman http://orcid.org/0000-0002-2215-5535
Nip, Ka Ming

Chu, Justin

Birol, Inanc
Funding

Funding for this research was provided by:

National Human Genome Research Institute (R01HG007182)

Genome Canada (BCB2 - 251LRD)
License Information

Text and Data Mining valid from 2018-09-10

Version of Record valid from 2018-09-10
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Article History

Received: 24 January 2018

Accepted: 31 August 2018

First Online: 10 September 2018

Ethics approval and consent to participate

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: The authors declare that they have no competing interests.

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